Hereditary Motor And Sensory Neuropathy, Type IIC [Supplementary Concept]
mutation in TRPV4
Date introduced: November 5, 2012
MeSH Unique ID: C565261
Heading Mapped to:
Entry Terms:
- Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2C
- HMSN2C
- Charcot-Marie-Tooth Neuropathy, Type 2C
- CMT2C
- HMSN IIC